List of variants in gene APC reported as not provided for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.5363G>A (p.Arg1788His)	rs201472075	0.00002
NM_000038.6(APC):c.220+2T>C	rs587781809
NM_000038.6(APC):c.2624dup (p.Arg876fs)	rs863225330
NM_000038.6(APC):c.2845A>G (p.Met949Val)	rs587781348
NM_000038.6(APC):c.3535T>C (p.Tyr1179His)	rs751249843
NM_000038.6(APC):c.4010_4013dup (p.Gln1338fs)	rs1131691256
NM_000038.6(APC):c.5803del (p.Gln1935fs)	rs1131691253
NM_000038.6(APC):c.994C>T (p.Arg332Ter)	rs775126020

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